rs786205106

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(CCTGTATATTCTTAAG;CCTGTATATTCTTAAG)	0	common in clinvar

Make rs786205106(-;-)

Make rs786205106(-;CCTGTATATTCTTAAG)

Reference

GRCh38.p2 38.2/146

Chromosome

1

Position

115740794

Gene

CASQ2

is a	snp
is	mentioned by
dbSNP	rs786205106
dbSNP (classic)	rs786205106
ClinGen	rs786205106
ebi	rs786205106
HLI	rs786205106
Exac	rs786205106
Gnomad	rs786205106
Varsome	rs786205106
LitVar	rs786205106
Map	rs786205106
PheGenI	rs786205106
Biobank	rs786205106
1000 genomes	rs786205106
hgdp	rs786205106
ensembl	rs786205106
geneview	rs786205106
scholar	rs786205106
google	rs786205106
pharmgkb	rs786205106
gwascentral	rs786205106
openSNP	rs786205106
23andMe	rs786205106
SNPshot	rs786205106
SNPdbe	rs786205106
MSV3d	rs786205106
GWAS Ctlg	rs786205106

Max Magnitude

0

ClinVar
Risk	rs786205106(-;-)
Alt	rs786205106(-;-)
Reference	Rs786205106(CCTGTATATTCTTAAG;CCTGTATATTCTTAAG)
Significance	Pathogenic
Disease	Ventricular tachycardia not provided
Variation	info
Gene	CASQ2
CLNDBN	Ventricular tachycardia, catecholaminergic polymorphic, 2 not provided
Reversed	1
HGVS	NC_000001.10:g.116283415_116283430del16
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000019177.28, RCV000170902.2,